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Completed

NCT Number: NCT06863922

A Pilot Study of Berberine (Soloways ™) in Patients with Type 2 Diabetes Mellitus Carrying TCF7L2 Polymorphisms

This pilot, genotype-stratified clinical trial aims to investigate the safety and preliminary efficacy of berberine supplementation in adult patients with type 2 diabetes mellitus (T2DM) who carry a specific high-risk TCF7L2 polymorphism (e.g., rs7903146) in the homozygous state. The study will compare improvements in glycemic control and metabolic markers between two groups: (1) homozygous carriers of the TCF7L2 "unfavorable" variant and (2) non-carriers (wild-type). It is hypothesized that berberine will yield greater reductions in HbA1c and fasting plasma glucose among homozygous carriers, potentially due to their distinct TCF7L2-mediated insulin secretion and sensitivity pathways.

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Key information

Age range

30 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for New Medical Technologies

Novosibirsk, 630090, Russia

About this study

Type 2 diabetes mellitus is driven by a combination of insulin resistance and impaired insulin secretion. Genetic polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene have been strongly associated with an increased risk of T2DM, potentially through altered beta-cell function and incretin signaling. Berberine, a natural alkaloid derived from plants such as Coptis chinensis, has demonstrated hypoglycemic effects by modulating pathways like AMPK, thereby improving insulin sensitivity and glucose metabolism. This pilot trial aims to clarify whether berberine offers a more pronounced metabolic benefit to individuals homozygous for a "high-risk" TCF7L2 polymorphism by targeting their unique pathophysiological mechanisms. Results will inform future larger-scale, genotype-focused interventional trials.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (age 30-70 years) with a confirmed diagnosis of type 2 diabetes mellitus.
  • On stable doses of metformin or other standard oral antihyperglycemic agents for at least 4 weeks prior to enrollment.
  • Willingness to undergo genetic testing for TCF7L2 polymorphisms. For the Homozygous Variant Cohort: confirmed homozygous high-risk TCF7L2 polymorphism (e.g., rs7903146) prior to enrollment.
  • For the Non-Variant Cohort: confirmed wild-type TCF7L2 genotype.

Exclusion criteria

  • Current use of insulin therapy or recent (within 4 weeks) change in diabetic medications.

Known hypersensitivity or intolerance to berberine or related compounds.

  • Significant renal or hepatic impairment.
  • Pregnancy or breastfeeding.
  • Any other acute or chronic condition that, in the investigator's judgment, could compromise the patient's safety or the study's integrity.

Treatment and study plan

Berberine

Dietary Supplement

Berberine 500-1000 mg, administered 2-3 times per day for 12 weeks, in addition to standard of care

Primary outcomes

  1. Change in Glycated Hemoglobin (HbA1c)

    Time frame: 12 weeks

  2. Change in Fasting Plasma Glucose (FPG)

    Time frame: 12 weeks

Secondary outcomes

  1. Change in HOMA-IR (Insulin Resistance Index)

    Time frame: 12 weeks

  2. Number of Adverse Events

    Time frame: 12 weeks

  3. Change in Lipid Profile Triglyceride

    Time frame: 12 weeks

  4. Change in Lipid Profile LDL-C

    Time frame: 12 weeks

  5. Change in Lipid Profile HDL-C

    Time frame: 12 weeks

  6. Change in Body Weight or Body Mass Index (BMI)

    Time frame: 12 weeks

  7. Change in Patient-Reported Quality of Life as Measured by the World Health Organization

    Time frame: 12 weeks

    Patient-reported quality of life will be assessed using the World Health Organization Quality of Life Instrument, Short Form (WHOQOL-BREF). This validated questionnaire provides scores ranging from 0 to 100 for each domain (physical health, psychological health, social relationships, and environment), where higher scores indicate a better quality of life. The outcome will be reported as the mean change in the relevant domain scores from baseline to 12 weeks.

Sponsors and collaborators

Lead sponsor

S.LAB (SOLOWAYS)

Other

Collaborators

  • Center for New Medical Technologies, Novosibirsk, Russia

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Mar 7, 2025
Registry last updated
Mar 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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